Variant #0000678589 (NC_000009.11:g.139089436C>G, NM_178138.4:c.929G>C (LHX3))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.139089436C>G
DNA change (hg38) -
Published as LHX3(NM_014564.4):c.944G>C (p.R315P), LHX3(NM_014564.5):c.944G>C (p.R315P)
ISCN -
DB-ID LHX3_000001 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00066 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LHX3 NM_014564.3 ?/. - c.944G>C r.(?) p.(Arg315Pro)
LHX3 NM_178138.4 ?/. - c.929G>C r.(?) p.(Arg310Pro)


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